Soybean variety 0007583

ABSTRACT

The instant invention relates to the novel soybean variety designated 0007583. Provided by the invention are the seeds, plants and derivatives of the soybean variety 0007583. Also provided by the invention are tissue cultures of the soybean variety 0007583 and the plants regenerated therefrom. Still further provided by the invention are methods for producing soybean plants by crossing the soybean variety 0007583 with itself or another soybean variety and plants produced by such methods.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to the field of soybeanbreeding. In particular, the invention relates to the novel soybeanvariety 0007583.

2. Description of Related Art

There are numerous steps in the development of any novel, desirableplant germplasm. Plant breeding begins with the analysis and definitionof problems and weaknesses of the current germplasm, the establishmentof program goals, and the definition of specific breeding objectives.The next step is selection of germplasm that possess the traits to meetthe program goals. The goal is to combine in a single variety animproved combination of desirable traits from the parental germplasm.These important traits may include higher seed yield, resistance todiseases and insects, better stems and roots, tolerance to drought andheat, better agronomic quality, resistance to herbicides, andimprovements in compositional traits.

Choice of breeding or selection methods depends on the mode of plantreproduction, the heritability of the trait(s) being improved, and thetype of variety used commercially (e.g., F₁ hybrid variety, purelinevariety, etc.). For highly heritable traits, a choice of superiorindividual plants evaluated at a single location will be effective,whereas for traits with low heritability, selection should be based onmean values obtained from replicated evaluations of families of relatedplants. Popular selection methods commonly include pedigree selection,modified pedigree selection, mass selection, recurrent selection andbackcrossing.

The complexity of inheritance influences choice of the breeding method.Backcross breeding is used to transfer one or a few favorable genes fora highly heritable trait into a desirable variety. This approach hasbeen used extensively for breeding disease-resistant varieties (Bowerset al., 1992; Nickell and Bernard, 1992). Various recurrent selectiontechniques are used to improve quantitatively inherited traitscontrolled by numerous genes. The use of recurrent selection inself-pollinating crops depends on the ease of pollination, the frequencyof successful hybrids from each pollination, and the number of hybridoffspring from each successful cross.

Each breeding program should include a periodic, objective evaluation ofthe efficiency of the breeding procedure. Evaluation criteria varydepending on the goal and objectives, but should include gain fromselection per year based on comparisons to an appropriate standard,overall value of the advanced breeding lines, and number of successfulvarieties produced per unit of input (e.g., per year, per dollarexpended, etc.).

Promising advanced breeding lines are thoroughly tested and compared toappropriate standards in environments representative of the commercialtarget area(s) for generally three or more years. The best lines arecandidates for new commercial varieties. Those still deficient in a fewtraits may be used as parents to produce new populations for furtherselection.

These processes, which lead to the final step of marketing anddistribution, may take as much as eight to 12 years from the time thefirst cross is made. Therefore, development of new varieties is atime-consuming process that requires precise forward planning, efficientuse of resources, and a minimum of changes in direction.

A most difficult task is the identification of individuals that aregenetically superior, because for most traits the true genotypic valueis masked by other confounding plant traits or environmental factors.One method of identifying a superior plant is to observe its performancerelative to other experimental plants and to one or more widely grownstandard varieties. Single observations are generally inconclusive,while replicated observations provide a better estimate of geneticworth.

The goal of plant breeding is to develop new, unique and superiorsoybean varieties and hybrids. The breeder initially selects and crossestwo or more parental lines, followed by repeated selfing and selection,producing many new genetic combinations. Each year, the plant breederselects the germplasm to advance to the next generation. This germplasmis grown under unique and different geographical, climatic and soilconditions, and further selections are then made, during and at the endof the growing season. The varieties which are developed areunpredictable. This unpredictability is because the breeder's selectionoccurs in unique environments, with no control at the DNA level (usingconventional breeding procedures), and with millions of differentpossible genetic combinations being generated. A breeder of ordinaryskill in the art cannot predict the final resulting lines he develops,except possibly in a very gross and general fashion. The same breedercannot produce the same variety twice by using the exact same originalparents and the same selection techniques. This unpredictability resultsin the expenditure of large amounts of research monies to developsuperior new soybean varieties.

The development of new soybean varieties requires the development andselection of soybean varieties, the crossing of these varieties andselection of progeny from the superior hybrid crosses. The hybrid seedis produced by manual crosses between selected male-fertile parents orby using male sterility systems. Hybrids may be identified by usingcertain single locus traits such as pod color, flower color, pubescencecolor or herbicide resistance which indicate that the seed is truly ahybrid. Additional data on parental lines as well as the phenotype ofthe hybrid influence the breeder's decision whether to continue with thespecific hybrid cross.

Pedigree breeding and recurrent selection breeding methods are used todevelop varieties from breeding populations. Breeding programs combinedesirable traits from two or more varieties or various broad-basedsources into breeding pools from which varieties are developed byselfing and selection of desired phenotypes. The new varieties areevaluated to determine which have commercial potential.

Pedigree breeding is commonly used for the improvement ofself-pollinating crops. Two parents which possess favorable,complementary traits are crossed to produce an F₁. An F₂ population isproduced by selfing one or several F₁'s. Selection of the bestindividuals may begin in the F₂ population (or later depending upon thebreeders objectives); then, beginning in the F₃, the best individuals inthe best families can be selected. Replicated testing of families canbegin in the F₃ or F₄ generation to improve the effectiveness ofselection for traits with low heritability. At an advanced stage ofinbreeding (i.e., F₆ and F₇), the best lines or mixtures ofphenotypically similar lines are tested for potential release as newvarieties.

Mass and recurrent selections can be used to improve populations ofeither self- or cross-pollinating crops. A genetically variablepopulation of heterozygous individuals is either identified or createdby intercrossing several different parents. The best plants are selectedbased on individual superiority, outstanding progeny, or excellentcombining ability. The selected plants are intercrossed to produce a newpopulation in which further cycles of selection are continued.

Backcross breeding has been used to transfer genetic loci for simplyinherited, highly heritable traits into a desirable homozygous varietywhich is the recurrent parent. The source of the trait to be transferredis called the donor or nonrecurent parent. The resulting plant isexpected to have the attributes of the recurrent parent (e.g., variety)and the desirable trait transferred from the donor parent. After theinitial cross, individuals possessing the phenotype of the donor parentare selected and repeatedly crossed (backcrossed) to the recurrentparent. The resulting plant is expected to have the attributes of therecurrent parent (e.g., variety) and the desirable trait transferredfrom the donor parent.

The single-seed descent procedure in the strict sense refers to plantinga segregating population, harvesting a sample of one seed per plant, andusing the one-seed sample to plant the next generation. When thepopulation has been advanced from the F₂ to the desired level ofinbreeding, the plants from which lines are derived will each trace todifferent F₂ individuals. The number of plants in a population declineseach generation due to failure of some seeds to germinate or some plantsto produce at least one seed. As a result, not all of the F₂ plantsoriginally sampled in the population will be represented by a progenywhen generation advance is completed.

In a multiple-seed procedure, soybean breeders commonly harvest one ormore pods from each plant in a population and thresh them together toform a bulk. Part of the bulk is used to plant the next generation andpart is put in reserve. The procedure has been referred to as modifiedsingle-seed descent or the pod-bulk technique.

The multiple-seed procedure has been used to save labor at harvest. Itis considerably faster to thresh pods with a machine than to remove oneseed from each by hand for the single-seed procedure. The multiple-seedprocedure also makes it possible to plant the same number of seeds of apopulation each generation of inbreeding. Enough seeds are harvested tomake up for those plants that did not germinate or produce seed.

Descriptions of other breeding methods that are commonly used fordifferent traits and crops can be found in one of several referencebooks (e.g., Allard, 1960; Simmonds, 1979; Sneep et al., 1979; Fehr,1987a,b).

Proper testing should detect any major faults and establish the level ofsuperiority or improvement over current varieties. In addition toshowing superior performance, there must be a demand for a new varietythat is compatible with industry standards or which creates a newmarket. The introduction of a new variety will incur additional costs tothe seed producer, the grower, processor and consumer; for specialadvertising and marketing, altered seed and commercial productionpractices, and new product utilization. The testing preceding release ofa new variety should take into consideration research and developmentcosts as well as technical superiority of the final variety. Forseed-propagated varieties, it must be feasible to produce seed easilyand economically.

Soybean, Glycine max (L), is an important and valuable field crop. Thus,a continuing goal of plant breeders is to develop stable, high yieldingsoybean varieties that are agronomically sound. The reasons for thisgoal are to maximize the amount of grain produced on the land used andto supply food for both animals and humans. To accomplish this goal, thesoybean breeder must select and develop soybean plants that have thetraits that result in superior varieties.

SUMMARY OF THE INVENTION

One aspect of the present invention relates to seed of the soybeanvariety 0007583. The invention also relates to plants produced bygrowing the seed of the soybean variety 0007583, as well as thederivatives of such plants. As used herein, the term “plant” includesplant cells, plant protoplasts, plant cells of a tissue culture fromwhich soybean plants can be regenerated, plant calli, plant clumps, andplant cells that are intact in plants or parts of plants, such aspollen, flowers, seeds, pods, leaves, stems, and the like.

Another aspect of the invention relates to a tissue culture ofregenerable cells of the soybean variety 0007583, as well as plantsregenerated therefrom, wherein the regenerated soybean plant is capableof expressing all the physiological and morphological characteristics ofa plant grown from the soybean seed designated 0007583.

Yet another aspect of the current invention is a soybean plantcomprising a single locus conversion of the soybean variety 0007583,wherein the soybean plant is otherwise capable of expressing all thephysiological and morphological characteristics of the soybean variety0007583. In particular embodiments of the invention, the single locusconversion may comprise a transgenic gene which has been introduced bygenetic transformation into the soybean variety 0007583 or a progenitorthereof. In still other embodiments of the invention, the single locusconversion may comprise a dominant or recessive allele. The locusconversion may confer potentially any trait upon the single locusconverted plant, including herbicide resistance, insect resistance,resistance to bacterial, fungal, or viral disease, male fertility orsterility, and improved nutritional quality.

Still yet another aspect of the invention relates to a first generation(F₁) hybrid soybean seed produced by crossing a plant of the soybeanvariety 0007583 to a second soybean plant. Also included in theinvention are the F₁ hybrid soybean plants grown from the hybrid seedproduced by crossing the soybean variety 0007583 to a second soybeanplant. Still further included in the invention are the seeds of an F₁hybrid plant produced with the soybean variety 0007583 as one parent,the second generation (F₂) hybrid soybean plant grown from the seed ofthe F₁ hybrid plant, and the seeds of the F₂ hybrid plant.

Still yet another aspect of the invention is a method of producingsoybean seeds comprising crossing a plant of the soybean variety 0007583to any second soybean plant, including itself or another plant of thevariety 0007583. In particular embodiments of the invention, the methodof crossing comprises the steps of a) planting seeds of the soybeanvariety 0007583; b) cultivating soybean plants resulting from said seedsuntil said plants bear flowers; c) allowing fertilization of the flowersof said plants; and, d) harvesting seeds produced from said plants.

Still yet another aspect of the invention is a method of producinghybrid soybean seeds comprising crossing the soybean variety 0007583 toa second, distinct soybean plant which is nonisogenic to the soybeanvariety 0007583. In particular embodiments of the invention, thecrossing comprises the steps of a) planting seeds of soybean variety0007583 and a second, distinct soybean plant, b) cultivating the soybeanplants grown from the seeds until the plants bear flowers; c) crosspollinating a flower on one of the two plants with the pollen of theother plant, and d) harvesting the seeds resulting from the crosspollinating.

Still yet another aspect of the invention is a method for developing asoybean plant in a soybean breeding program comprising: obtaining asoybean plant, or its parts, of the variety 0007583; and b) employingsaid plant or parts as a source of breeding material using plantbreeding techniques. In the method, the plant breeding techniques may beselected from the group consisting of recurrent selection, massselection, bulk selection, backcrossing, pedigree breeding, geneticmarker-assisted selection and genetic transformation. In certainembodiments of the invention, the soybean plant of variety 0007583 isused as the male or female parent.

Still yet another aspect of the invention is a method of producing asoybean plant derived from the soybean variety 0007583, the methodcomprising the steps of: (a) preparing a progeny plant derived fromsoybean variety 0007583 by crossing a plant of the soybean variety0007583 with a second soybean plant, wherein a sample of the seed of thesoybean variety 0007583 was deposited under ATCC Accession No. PTA-5764;and (b) crossing the progeny plant with itself or a second plant toproduce a progeny plant of a subsequent generation which is derived froma plant of the soybean variety 0007583. In one embodiment of theinvention, the method further comprises: (c) crossing the progeny plantof a subsequent generation with itself or a second plant; and (d)repeating steps (b) and (c) for at least 2–10 additional generations toproduce an inbred soybean plant derived from the soybean variety0007583. Also provided by the invention is a plant produced by this andthe other methods of the invention. Plant variety 0007583-derived plantsproduced by this and the other methods of the invention described hereinmay, in certain embodiments of the invention, be further defined ascomprising at least two, including at least three, four, six, eight andtwelve of the traits of plant variety 0007583 given in Table 1.

In one embodiment of the invention, the method of producing a soybeanplant derived from the soybean variety 0007583 may be still furtherdefined as a method of producing a soybean plant with increased seed oilcontent, wherein the inbred soybean plant comprises increased seed oilcontent relative to the second soybean plant. In another embodiment ofthe invention, the method may be further defined as a method ofproducing a soybean plant with increased protein content, wherein theinbred soybean plant comprises increased seed protein content relativeto the second soybean plant. In a still further embodiment of theinvention, the method may be further defined as a method of producing asoybean plant with increased seed oil and protein content, wherein theinbred soybean plant comprises increased seed oil and protein contentrelative to said second soybean plant.

In another embodiment of the invention, the method of producing asoybean plant derived from the soybean variety 0007583 furthercomprises: (a) crossing the soybean variety 0007583-derived soybeanplant with itself or another soybean plant to yield additional soybeanvariety 0007583-derived progeny soybean seed; (b) growing the progenysoybean seed of step (a) under plant growth conditions, to yieldadditional soybean variety 0007583-derived soybean plants; and (c)repeating the crossing and growing steps of (a) and (b) from 0 to 7times to generate further soybean variety 0007583-derived soybeanplants. The invention still further provides a soybean plant produced bythis and the foregoing methods.

DETAILED DESCRIPTION OF THE INVENTION

The instant invention provides methods and composition relating toplants, seeds and derivatives of the soybean variety 0007583. Soybeanvariety 0007583 is adapted to the mid-group 2 soybean growing region, isresistance to multiple Phytophthora races and exhibits high seed oil andprotein in combination with high yield. The variety was derived from thecross of soybean varieties A2552 and SN30003. The original cross ofA2552 and SN30003 was made at Isabella, PR during the winter of 1996–97.F1 seed was grown at Janesville, WI in 1997 and F2 seed was grown atIsabella, PR during the winter of 1997–98. Bulked F3 seed was grown atJanesville, Wis. in 1998 and single plant selections were made from thebulk population and threshed individually. F3:4 seed was planted in PRYT(Single Plant Yield Test) in 1999 at Janesville, Wis. F3:5 seed wasplanted at 5 locations in Wisconsin in 2000 to test for yield andgenotype while breeder seed was grown at Beaman, Iowa. F3:6 seed wasplanted at 11 locations throughout the Midwest in 2001 to test for yieldand genotype while breeder seed was increased at Beaman, Iowa. Some ofthe criteria used to select the variety in various generations include:seed yield, lodging resistance, emergence, seedling vigor, diseasetolerance, maturity, plant height and seed oil and protein content.

The soybean variety 0007583 has been judged to be uniform for breedingpurposes and testing. The variety 0007583 can be reproduced by plantingand growing seeds of the variety under self-pollinating orsib-pollinating conditions, as is known to those of skill in theagricultural arts. Variety 0007583 shows no variants other than whatwould normally be expected due to environment or that would occur foralmost any characteristic during the course of repeated sexualreproduction. The results of an objective description of the variety arepresented below, in Table 1. Those of skill in the art will recognizethat these are typical values that may vary due to environment and thatother values that are substantially equivalent are within the scope ofthe invention.

TABLE 1 Phenotypic Description of Variety 0007583 Trait PhenotypeRelative Maturity 2.7 Roundup Ready Suscept. STS Suscept. LibertySuscept. Flower Purple Pubescence Gray Hilum Impperfect Black Pod ColorTan Seed Luster Dull Hypocotyl Color Light Purple Seed Shape SphericalFlattened Leaf Shape Ovate Leaflet Size Medium Leaf Color Medium CanopyBushy Growth Habit Indeterminate Phytophthora Allele Rps1^(k) SCN Race 3Susc. SCN Race 14 Susc. Area of adaptation: Mid-group 2 soybean growingregion. PRR tolerance score 4.7 (test average of 4.7) IDC compositescore 4.3 (test average of 4.7).

The performance characteristics of soybean variety 0007583 were alsoanalyzed and comparisons were made with competing varieties.Characteristics examined included maturity, plant height, lodging, seedprotein and oil content and iron deficiency chlorosis rating. Theresults of the analysis are presented below, in Tables 2–7.

TABLE 2 Exemplary Agronomic Traits of Variety 0007583 and SelectedVarieties Variety Mat Date Ht Lodg Protein Oil 0007583 24.5 37.5 2.546.2 20.4 A2247 23.0 34.5 2.5 43.3 21.6 A2553 24.5 31.0 2.5 40.2 23.0A2824 29.0 33.0 3.0 44.0 21.2 SN30003 24.5 37.0 2.5 51.0 18.5 SN3001727.5 42.0 3.0 49.1 19.7

TABLE 3 Iron Deficiency Chlorosis Rating for Variety 0007583 andSelected Varieties Variety IDE IDC Mean 0007583 4.7 6.3 5.5 A1923 3.34.0 3.7 A2247 4.7 4.5 4.6 A2553 4.7 5.0 4.8 Mean 4.4 5.0 4.7 Range2.7–6.2 2.8–7.2 2.8–6.5 IDE = Early iron deficiency chlorosis rating IDC= Iron deficiency chlorosis rating

TABLE 4 Yield Testing for Variety 0007583 Gen. Year Test-Entry #locsRank #Entries F₄ 1999 9WY37M-02 1 13 48 F₅ 2000 00JWIX-10 5 01 50 F₆2001 01JWH0-21 11 32 50

TABLE 5 Head to Head Comparisons of Variety 0007583 (Check) VersusListed Others: All Year, All Location BU/AC BU/AC MAT MAT MAT IDE IDEIDE OIL VARIETY TST WINS CHK CMP DIFF #TST CHK CMP #TST CHK CMP #TSTAG2102-14 11 9 47.4 43.9 3.5 9 25.6 20.6 2 4.3 4.8 4 AG2202 11 7 47.447.2 0.2 9 25.6 24.3 2 4.3 4.8 4 A2247 15 10 49.4 47.1 2.3 11 25.4 22.62 4.3 4.8 7 AG2402 11 7 47.4 45.3 2.1 9 25.6 23.8 2 4.3 4.1 4 A2553 15 249.4 53.0 −3.6 11 25.4 25.4 2 4.3 4.4 7 CSR2310 11 3 47.4 48.4 −1.0 925.6 24.6 2 4.3 4.6 4 CST21000 11 4 47.4 49.5 −2.1 9 25.6 24.4 2 4.3 4.84 CST23000 11 2 47.4 50.4 −3.0 9 25.6 26.1 2 4.3 4.4 4 CST231N 11 4 47.448.5 −1.1 9 25.6 23.2 2 4.3 4.3 4 MBS59125 11 3 47.4 49.1 −1.7 9 25.629.3 2 4.3 4.3 4 NKS24-L2 11 5 47.4 48.4 −1.0 9 25.6 22.5 2 4.3 3.6 4PION92B23 11 5 47.4 48.1 −0.6 9 25.6 21.9 2 4.3 3.8 3 PION92B35 11 447.4 47.8 −0.3 9 25.6 23.1 2 4.3 5.4 4 OIL OIL PRO PRO PRO PHT PHT PHTLDG LDG LDG CHK CMP #TST CHK CMP #TST CHK CMP #TST CHK CMP AG2102-1420.9 22.2 4 44.3 40.0 6 37.0 31.8 9 1.9 1.3 AG2202 20.9 21.4 4 44.3 40.36 37.0 34.3 9 1.9 1.2 A2247 20.8 22.0 7 44.8 41.9 8 37.1 35.4 11  2.02.0 AG2402 20.9 22.1 4 44.3 40.8 6 37.0 35.3 9 1.9 1.6 A2553 20.8 23.1 744.8 38.9 8 37.1 33.1 11  2.0 1.8 CSR2310 20.9 21.5 4 44.3 40.7 6 37.033.5 9 1.9 1.5 CST21000 20.9 22.2 4 44.3 40.4 6 37.0 31.3 9 1.9 1.2CST23000 20.9 21.7 4 44.3 40.1 6 37.0 35.1 9 1.9 1.4 CST231N 20.9 21.8 444.3 41.6 6 37.0 33.6 9 1.9 1.4 MBS59125 20.9 20.4 4 44.3 40.9 6 37.035.2 9 1.9 1.9 NKS24-L2 20.9 21.9 4 44.3 39.9 6 37.0 32.2 9 1.9 1.6PION92B23 21.0 22.7 3 43.9 38.9 6 37.0 31.4 9 1.9 1.8 PION92B35 20.922.0 4 44.3 40.8 6 37.0 35.4 9 1.9 2.2 TST = Research-No. of tests WINS= Number of wins versus listed varieties BU/AC = Yield (bushels/acre)MAT = Maturity Date (days) IDE = Iron deficiency chlorosis (early)rating OIL = Seed oil content PRO = Seed protein content PHT = PlantHeight (inches) LDG = Lodging Rating (scale: 1–9, 1 = best)

TABLE 6 Performance Comparison of Variety 0007583 Versus CompetingVarieties MAT PLT PHO FLD % % Variety YLD DATE HGT LDG SCR EMR IDC PROOIL 0007583 47.4 25.6 37.0 1.9 3.3 1.3 4.3 43.8 21.2 ASGROW A2553 52.925.6 33.8 1.6 2.5 1.8 4.4 38.8 23.1 DEKALB DKB23-95 51.3 25.4 33.5 1.53.0 1.3 5.1 42.2 21.4 STINE 2491-6 50.8 26.7 32.5 1.4 2.9 1.7 4.8 42.121.2 CORN STATES T23000 50.4 26.1 35.1 1.4 2.8 1.3 4.4 40.3 21.9 CORNSTATES T21000 49.5 24.4 31.3 1.2 2.5 1.5 4.8 40.6 22.3 MIKE BRAYTONSEEDS 59125 49.1 29.3 35.2 1.9 2.9 1.3 4.3 41.2 20.5 PIONEER 92B37 48.522.0 39.4 2.1 3.8 1.7 4.2 40.8 22.4 DEKALB DKB23-73 48.5 23.2 33.6 1.42.9 1.2 4.3 41.9 21.9 DEKALB DKB23-51 48.4 24.6 33.5 1.5 2.9 2.0 4.641.0 21.6 SYNGENTA NKS24-L2 48.4 22.5 32.2 1.6 3.2 1.2 3.6 40.1 22.0PIONEER 92B23 48.1 21.9 31.4 1.8 3.2 1.3 3.8 39.5 22.7 PIONEER 92B3547.8 23.1 35.4 2.2 2.8 1.5 5.4 41.0 22.1 ASGROW AG2202 47.2 24.3 34.31.2 2.4 1.8 4.8 40.6 21.5 ASGROW A2247 46.2 22.5 35.8 1.9 3.5 1.5 4.841.9 22.2 STINE 1892-2 46.0 18.2 31.1 2.3 3.7 1.7 4.2 40.6 22.7 SYNGENTANKS21-A1 45.9 17.6 31.6 1.8 3.3 2.0 5.2 40.3 22.7 HISOY 10C2-1-2 45.519.8 34.1 2.0 3.6 1.4 5.0 40.5 21.7 IVORY 45.3 20.6 29.5 1.2 3.3 1.3 4.841.6 22.2 HISOY 10C2-1-3 45.3 18.9 36.9 1.9 3.6 1.5 4.1 40.6 21.8 ASGROWAG2402 45.3 23.8 35.3 1.6 2.7 1.5 4.1 41.0 22.2 HISOY 10C2-13-2 45.125.1 34.2 2.1 3.3 1.0 4.5 41.2 22.2 ASGROW A2069 45.0 18.0 30.5 1.6 3.21.3 3.8 41.4 21.7 ASGROW A1923 44.5 17.3 31.8 1.2 2.9 1.5 4.7 40.6 22.0ASGROW AG2001 43.7 18.3 32.3 1.6 2.9 1.2 5.1 41.2 23.0 DEKALB DKB19-5142.3 18.3 32.0 1.2 2.8 2.2 4.1 39.5 22.6 ENTRY MEAN 48.2 23.3 33.9 1.83.1 1.5 4.7 40.9 21.9 LSD (.30) 1.4 0.8 1.1 0.3 0.3 0.4 0.8 0.4 0.2 LSD(.05) 2.7 1.6 2.1 0.6 0.6 0.8 1.5 0.8 0.4 CV 6.7 7.3 5.4 34.3 19.0 34.316.5 1.5 1.4 # of TESTS 11.0 9.0 6.0 9.0 8.0 3.0 2.0 5.0 5.0

TABLE 7 Additional Comparison of 0007583 With Selected Varieties Over 5Locations MAT PLT PHO Variety YLD DATE HGT LDG SCR % PRO % OIL 000758354.7 24.5 37.5 2.5 4.5 46.2 20.4 ASGROW 53.1 24.5 31.0 2.5 3.5 40.2 23.0A2553 ASGROW 49.7 23.0 34.5 2.5 3.5 43.3 21.6 A2247 ASGROW 49.5 29.033.0 3.0 5.0 44.0 21.2 A2824 SN30017 46.7 27.5 42.0 3.0 5.5 49.1 19.7SN30003 44.4 24.5 37.5 2.5 5.0 50.5 18.7 ENTRY 45.8 25.1 37.0 2.6 4.947.0 19.7 MEAN LSD (.30) 2.8 1.3 1.9 0.5 0.7 0.8 0.4 LSD (.05) 5.3 2.43.7 1.0 1.3 1.5 0.7 CV 8.2 4.8 5.0 19.3 12.8 2.2 2.5 # of TESTS 4.0 2.02.0 2.0 2.0 4.0 4.0I. Breeding Soybean Variety 0007583

One aspect of the current invention concerns methods for crossing thesoybean variety 0007583 with itself or a second plant and the seeds andplants produced by such methods. These methods can be used forpropagation of the soybean variety 0007583, or can be used to producehybrid soybean seeds and the plants grown therefrom. Hybrid soybeanplants can be used by farmers in the commercial production of soyproducts or may be advanced in certain breeding protocols for theproduction of novel soybean varieties. A hybrid plant can also be usedas a recurrent parent at any given stage in a backcrossing protocolduring the production of a single locus conversion of the soybeanvariety 0007583.

The variety of the present invention is well suited to the developmentof new varieties based on the elite nature of the genetic background ofthe variety, and particularly the high oil and protein content of thevariety in combination with high yield. In selecting a second plant tocross with 0007583 for the purpose of developing novel soybeanvarieties, it will typically be desired to choose those plants whicheither themselves exhibit one or more selected desirable characteristicsor which exhibit the desired characteristic(s) when in hybridcombination. Examples of potentially desired characteristics includeseed yield, lodging resistance, emergence, seedling vigor, diseasetolerance, maturity, plant height, high oil content, high proteincontent and shattering resistance.

Any time the soybean variety 0007583 is crossed with another, different,variety, first generation (F₁) soybean progeny are produced. The hybridprogeny are produced regardless of characteristics of the two varietiesproduced. As such, an F₁ hybrid soybean plant may be produced bycrossing 0007583 with any second soybean plant. The second soybean plantmay be genetically homogeneous (e.g., inbred) or may itself be a hybrid.Therefore, any F₁ hybrid soybean plant produced by crossing soybeanvariety 0007583 with a second soybean plant is a part of the presentinvention.

Soybean plants (Glycine max L.) can be crossed by either natural ormechanical techniques (see, e.g., Fehr, 1980). Natural pollinationoccurs in soybeans either by self pollination or natural crosspollination, which typically is aided by pollinating organisms. Ineither natural or artificial crosses, flowering and flowering time arean important consideration. Soybean is a short-day plant, but there isconsiderable genetic variation for sensitivity to photoperiod (Hamner,1969; Criswell and Hume, 1972). The critical day length for floweringranges from about 13 h for genotypes adapted to tropical latitudes to 24h for photoperiod-insensitive genotypes grown at higher latitudes(Shibles et al., 1975). Soybeans seem to be insensitive to day lengthfor 9 days after emergence. Photoperiods shorter than the critical daylength are required for 7 to 26 days to complete flower induction(Borthwick and Parker, 1938; Shanmugasundaram and Tsou, 1978).

Sensitivity to day length is an important consideration when genotypesare grown outside of their area of adaptation. When genotypes adapted totropical latitudes are grown in the field at higher latitudes, they maynot mature before frost occurs. Plants can be induced to flower andmature earlier by creating artificially short days or by grafting (Fehr,1980). Soybeans frequently are grown in winter nurseries located at sealevel in tropical latitudes where day lengths are much shorter thantheir critical photoperiod. The short day lengths and warm temperaturesencourage early flowering and seed maturation, and genotypes can producea seed crop in 90 days or fewer after planting. Early flowering isuseful for generation advance when only a few self-pollinated seeds perplant are needed, but not for artificial hybridization because theflowers self-pollinate before they are large enough to manipulate forhybridization. Artificial lighting can be used to extend the natural daylength to about 14.5 h to obtain flowers suitable for hybridization andto increase yields of self-pollinated seed.

The effect of a short photoperiod on flowering and seed yield can bepartly offset by altitude, probably due to the effects of cooltemperature (Major et al., 1975). At tropical latitudes, varietiesadapted to the northern U.S. perform more like those adapted to thesouthern U.S. at high altitudes than they do at sea level.

The light level required to delay flowering is dependent on the qualityof light emitted from the source and the genotype being grown. Bluelight with a wavelength of about 480 nm requires more than 30 times theenergy to inhibit flowering as red light with a wavelength of about 640nm (Parker et al., 1946).

Temperature can also play a significant role in the flowering anddevelopment of soybean (Major et al., 1975). It can influence the timeof flowering and suitability of flowers for hybridization. Temperaturesbelow 21° C. or above 32° C. can reduce floral initiation or seed set(Hamner, 1969; van Schaik and Probst, 1958). Artificial hybridization ismost successful between 26° C. and 32° C. because cooler temperaturesreduce pollen shed and result in flowers that self-pollinate before theyare large enough to manipulate. Warmer temperatures frequently areassociated with increased flower abortion caused by moisture stress;however, successful crosses are possible at about 35° C. if soilmoisture is adequate.

Soybeans have been classified as indeterminate, semi-determinate, anddeterminate based on the abruptness of stem termination after floweringbegins (Bernard and Weiss, 1973). When grown at their latitude ofadaptation, indeterminate genotypes flower when about one-half of thenodes on the main stem have developed. They have short racemes with fewflowers, and their terminal node has only a few flowers.Semi-determinate genotypes also flower when about one-half of the nodeson the main stem have developed, but node development and flowering onthe main stem stops more abruptly than on indeterminates. Their racemesare short and have few flowers, except for the terminal one, which mayhave several times more flowers than those lower on the plant.Determinate varieties begin flowering when all or most of the nodes onthe main stem have developed. They usually have elongated racemes thatmay be several centimeters in length and may have a large number offlowers. Stem termination and flowering habit are reported to becontrolled by two major genes (Bernard and Weiss, 1973).

Soybean flowers typically are self-pollinated on the day the corollaopens. The amount of natural crossing, which is typically associatedwith insect vectors such as honeybees, is approximately 1% for adjacentplants within a row and 0.5% between plants in adjacent rows. Thestructure of soybean flowers is similar to that of other legume speciesand consists of a calyx with five sepals, a corolla with five petals, 10stamens, and a pistil (Carlson, 1973). The calyx encloses the corollauntil the day before anthesis. The corolla emerges and unfolds to exposea standard, two wing petals, and two keel petals. An open flower isabout 7 mm long from the base of the calyx to the tip of the standardand 6 mm wide across the standard. The pistil consists of a single ovarythat contains one to five ovules, a style that curves toward thestandard, and a club-shaped stigma. The stigma is receptive to pollenabout 1 day before anthesis and remains receptive for 2 days afteranthesis, if the flower petals are not removed. Filaments of ninestamens are fused, and the one nearest the standard is free. The stamensform a ring below the stigma until about 1 day before anthesis, thentheir filaments begin to elongate rapidly and elevate the anthers aroundthe stigma. The anthers dehisce on the day of anthesis, pollen grainsfall on the stigma, and within 10 h the pollen tubes reach the ovary andfertilization is completed (Johnson and Bernard, 1963).

Self-pollination occurs naturally in soybean with no manipulation of theflowers. For the crossing of two soybean plants, it is typicallypreferable, although not required, to utilize artificial hybridization.In artificial hybridization, the flower used as a female in a cross ismanually cross pollinated prior to maturation of pollen from the flower,thereby preventing self fertilization, or alternatively, the male partsof the flower are emasculated using a technique known in the art.Techniques for emasculating the male parts of a soybean flower include,for example, physical removal of the male parts, use of a genetic factorconferring male sterility, and application of a chemical gametocide tothe male parts.

For artificial hybridization employing emasculation, flowers that areexpected to open the following day are selected on the female parent.The buds are swollen and the corolla is just visible through the calyxor has begun to emerge. Usually no more than two buds on a parent plantare prepared, and all self-pollinated flowers or immature buds areremoved with forceps. Special care is required to remove immature budsthat are hidden under the stipules at the leaf axil, and could developinto flowers at a later date. The flower is grasped between the thumband index finger and the location of the stigma determined by examiningthe sepals. A long, curvy sepal covers the keel, and the stigma is onthe opposite side of the flower. The calyx is removed by grasping asepal with the forceps, pulling it down and around the flower, andrepeating the procedure until the five sepals are removed. The exposedcorolla is removed by grasping it just above the calyx scar, thenlifting and wiggling the forceps simultaneously. Care is taken to graspthe corolla low enough to remove the keel petals without injuring thestigma. The ring of anthers is visible after the corolla is removed,unless the anthers were removed with the petals. Cross-pollination canthen be carried out using, for example, petri dishes or envelopes inwhich male flowers have been collected. Desiccators containing calciumchloride crystals are used in some environments to dry male flowers toobtain adequate pollen shed.

It has been demonstrated that emasculation is unnecessary to preventself-pollination (Walker et al., 1979). When emasculation is not used,the anthers near the stigma frequently are removed to make it clearlyvisible for pollination. The female flower usually is hand-pollinatedimmediately after it is prepared; although a delay of several hours doesnot seem to reduce seed set. Pollen shed typically begins in the morningand may end when temperatures are above 30° C., or may begin later andcontinue throughout much of the day with more moderate temperatures.

Pollen is available from a flower with a recently opened corolla, butthe degree of corolla opening associated with pollen shed may varyduring the day. In many environments, it is possible to collect maleflowers and use them immediately without storage. In the southern U.S.and other humid climates, pollen shed occurs in the morning when femaleflowers are more immature and difficult to manipulate than in theafternoon, and the flowers may be damp from heavy dew. In thosecircumstances, male flowers are collected into envelopes or petri dishesin the morning and the open container is typically placed in adesiccator for about 4 h at a temperature of about 25° C. The desiccatormay be taken to the field in the afternoon and kept in the shade toprevent excessive temperatures from developing within it. Pollenviability can be maintained in flowers for up to 2 days when stored atabout 5° C. In a desiccator at 3° C., flowers can be stored successfullyfor several weeks; however, varieties may differ in the percentage ofpollen that germinates after long-term storage (Kuehl, 1961).

Either with or without emasculation of the female flower, handpollination can be carried out by removing the stamens and pistil with aforceps from a flower of the male parent and gently brushing the anthersagainst the stigma of the female flower. Access to the stamens can beachieved by removing the front sepal and keel petals, or piercing thekeel with closed forceps and allowing them to open to push the petalsaway. Brushing the anthers on the stigma causes them to rupture, and thehighest percentage of successful crosses is obtained when pollen isclearly visible on the stigma. Pollen shed can be checked by tapping theanthers before brushing the stigma. Several male flowers may have to beused to obtain suitable pollen shed when conditions are unfavorable, orthe same male may be used to pollinate several flowers with good pollenshed.

When male flowers do not have to be collected and dried in a desiccator,it may be desired to plant the parents of a cross adjacent to eachother. Plants usually are grown in rows 65 to 100 cm apart to facilitatemovement of personnel within the field nursery. Yield of self-pollinatedseed from an individual plant may range from a few seeds to more than1,000 as a function of plant density. A density of 30 plants/m of rowcan be used when 30 or fewer seeds per plant is adequate, 10 plants/mcan be used to obtain about 100 seeds/plant, and 3 plants/m usuallyresults in maximum seed production per plant. Densities of 12 plants/mor less commonly are used for artificial hybridization.

Multiple planting dates about 7 to 14 days apart usually are used tomatch parents of different flowering dates. When differences inflowering dates are extreme between parents, flowering of the laterparent can be hastened by creating an artificially short day orflowering of the earlier parent can be delayed by use of artificiallylong days or delayed planting. For example, crosses with genotypesadapted to the southern U.S. are made in northern U.S. locations bycovering the late genotype with a box, large can, or similar containerto create an artificially short photoperiod of about 12 h for about 15days beginning when there are three nodes with trifoliate leaves on themain stem. Plants induced to flower early tend to have flowers thatself-pollinate when they are small and can be difficult to prepare forhybridization.

Grafting can be used to hasten the flowering of late floweringgenotypes. A scion from a late genotype grafted on a stock that hasbegun to flower will begin to bloom up to 42 days earlier than normal(Kiihl et al., 1977). First flowers on the scion appear from 21 to 50days after the graft.

Genetic male sterility is available in soybeans and may be useful tofacilitate hybridization in the context of the current invention,particularly for recurrent selection programs (Brim and Stuber, 1973).The distance required for complete isolation of a crossing block is notclear; however, outcrossing is less than 0.5% when male-sterile plantsare 12 m or more from a foreign pollen source (Boerma and Moradshahi,1975). Plants on the boundaries of a crossing block probably sustain themost outcrossing with foreign pollen and can be eliminated at harvest tominimize contamination.

Cross-pollination is more common within rows than between adjacent rows;therefore, it may be preferable to grow populations with genetic malesterility on a square grid to create rows in all directions. Forexample, single-plant hills on 50-cm centers may be used, withsubdivision of the area into blocks of an equal number of hills forharvest from bulks of an equal amount of seed from male-sterile plantsin each block to enhance random pollination.

Observing pod development 7 days after pollination generally is adequateto identify a successful cross. Abortion of pods and seeds can occurseveral weeks after pollination, but the percentage of abortion usuallyis low if plant stress is minimized (Shibles et al., 1975). Pods thatdevelop from artificial hybridization can be distinguished fromself-pollinated pods by the presence of the calyx scar, caused byremoval of the sepals. The sepals begin to fall off as the pods mature;therefore, harvest should be completed at or immediately before the timethe pods reach their mature color. Harvesting pods early also avoids anyloss by shattering.

Once harvested, pods are typically air-dried at not more than 38° C.until the seeds contain 13% moisture or less, then the seeds are removedby hand. Seed can be stored satisfactorily at about 25° C. for up to ayear if relative humidity is 50% or less. In humid climates, germinationpercentage declines rapidly unless the seed is dried to 7% moisture andstored in an air-tight container at room temperature. Long-term storagein any climate is best accomplished by drying seed to 7% moisture andstoring it at 10° C. or less in a room maintained at 50% relativehumidity or in an air-tight container.

II. Single Locus Conversions

When the term soybean variety 0007583 is used in the context of thepresent invention, this also includes any single locus conversions ofthat variety. The term single locus converted plant as used hereinrefers to those soybean plants which are developed by a plant breedingtechnique called backcrossing, wherein essentially all of the desiredmorphological and physiological characteristics of a variety arerecovered in addition to the single locus transferred into the varietyvia the backcrossing technique. Backcrossing methods can be used withthe present invention to improve or introduce a characteristic into thepresent variety. The term backcrossing as used herein refers to therepeated crossing of a hybrid progeny back to one of the parentalsoybean plants for that hybrid. The parental soybean plant whichcontributes the locus for the desired characteristic is termed thenonrecurrent or donor parent. This terminology refers to the fact thatthe nonrecurrent parent is used one time in the backcross protocol andtherefore does not recur. The parental soybean plant to which the locusor loci from the nonrecurrent parent are transferred is known as therecurrent parent as it is used for several rounds in the backcrossingprotocol (Poehlman et al., 1995; Fehr, 1987a,b; Sprague and Dudley,1988).

In a typical backcross protocol, the original variety of interest(recurrent parent) is crossed to a second variety (nonrecurrent parent)that carries the single locus of interest to be transferred. Theresulting progeny from this cross are then crossed again to therecurrent parent and the process is repeated until a soybean plant isobtained wherein essentially all of the desired morphological andphysiological characteristics of the recurrent parent are recovered inthe converted plant, in addition to the single transferred locus fromthe nonrecurrent parent.

The selection of a suitable recurrent parent is an important step for asuccessful backcrossing procedure. The goal of a backcross protocol isto alter or substitute a single trait or characteristic in the originalvariety. To accomplish this, a single locus of the recurrent variety ismodified or substituted with the desired locus from the nonrecurrentparent, while retaining essentially all of the rest of the desiredgenetic, and therefore the desired physiological and morphologicalconstitution of the original variety. The choice of the particularnonrecurrent parent will depend on the purpose of the backcross; one ofthe major purposes is to add some commercially desirable, agronomicallyimportant trait to the plant. The exact backcrossing protocol willdepend on the characteristic or trait being altered to determine anappropriate testing protocol. Although backcrossing methods aresimplified when the characteristic being transferred is a dominantallele, a recessive allele may also be transferred. In this instance itmay be necessary to introduce a test of the progeny to determine if thedesired characteristic has been successfully transferred.

Soybean varieties can also be developed from more than two parents(Fehr, 1987a). The technique, known as modified backcrossing, usesdifferent recurrent parents during the backcrossing. Modifiedbackcrossing may be used to replace the original recurrent parent with avariety having certain more desirable characteristics or multipleparents may be used to obtain different desirable characteristics fromeach.

Many single locus traits have been identified that are not regularlyselected for in the development of a new inbred but that can be improvedby backcrossing techniques. Single locus traits may or may not betransgenic; examples of these traits include, but are not limited to,male sterility, herbicide resistance, resistance to bacterial, fungal,or viral disease, insect resistance, restoration of male fertility,enhanced nutritional quality, yield stability, and yield enhancement.These comprise genes generally inherited through the nucleus.

Direct selection may be applied where the single locus acts as adominant trait. An example of a dominant trait is the herbicideresistance trait. For this selection process, the progeny of the initialcross are sprayed with the herbicide prior to the backcrossing. Thespraying eliminates any plants which do not have the desired herbicideresistance characteristic, and only those plants which have theherbicide resistance gene are used in the subsequent backcross. Thisprocess is then repeated for all additional backcross generations.

One type of single locus trait having particular utility is a gene whichconfers resistance to the herbicide glyphosate. Glyphosate inhibits theaction of the enzyme EPSPS, which is active in the biosynthetic pathwayof aromatic amino acids. Inhibition of this enzyme leads to starvationfor the amino acids phenylalanine, tyrosine, and tryptophan andsecondary metabolites derived therefrom. Mutants of this enzyme areavailable which are resistant to glyphosate. For example, U.S. Pat. No.4,535,060 describes the isolation of EPSPS mutations which conferglyphosate resistance upon organisms having the Salmonella typhimuriumgene for EPSPS, termed aroA. A mutant EPSPS gene having similarmutations also has been cloned from Zea mays. The mutant gene encodes aprotein with amino acid changes at residues 102 and 106. When these orother similar genes are introduced into a plant by genetictransformation, a herbicide resistant phenotype results.

Plants having inherited a transgene comprising a mutated EPSPS gene maybe directly treated with the herbicide glyphosate without the result ofsignificant damage to the plant. This phenotype provides farmers withthe benefit of controlling weed growth in a field of plants having theherbicide resistance trait by application of the broad spectrumherbicide glyphosate. For example, one could apply the herbicideROUNDUP™, a commercial formulation of glyphosate manufactured and soldby the Monsanto Company, over the top in fields where the glyphosateresistant soybeans are grown. The herbicide application rates may rangefrom about 4 ounces of ROUNDUP™ to about 256 ounces ROUNDUP™ per acre.More preferably, about 16 ounces to about 64 ounces per acre of ROUNDUP™may be applied to the field. However, the application rate may beincreased or decreased as needed, based on the abundance and/or type ofweeds being treated. Additionally, depending on the location of thefield and weather conditions, which will influence weed growth and thetype of weed infestation, it may be desirable to conduct furtherglyphosate treatments. The second glyphosate application will alsotypically comprise an application of about 16 ounces to about 64 ouncesof ROUNDUP™ per acre treated. Again, the treatment rate may be adjustedbased on field conditions. Such methods of application of herbicides toagricultural crops are well known in the art and are summarized ingeneral in Anderson, 1983.

It will be understood to those of skill in the art that a herbicideresistance gene locus may be used for direct selection of plants havingthe resistance gene. For example, by applying about 16 to 64 ounces ofROUNDUP™ per acre to a collection of soybean plants which either have orlack the herbicide resistance trait, the plants lacking the trait willbe killed or damaged. In this way, the herbicide resistant plants may beselected and used for commercial applications or advanced in certainbreeding protocols. This application may find particular use during thebreeding and development of herbicide resistant elite soybean varieties.

White flower color is an example of a recessive single locus trait. Inthis example, the progeny resulting from the first backcross generation(BC₁) are grown and selfed. The selfed progeny from the BC₁ plant aregrown to determine which BC₁ plants carry the recessive gene for whiteflower color. In other recessive traits, additional progeny testing, forexample growing additional generations such as the BC₁F₂, may berequired to determine which plants carry the recessive gene.

Selection of soybean plants for breeding is not necessarily dependent onthe phenotype of a plant and instead can be based on geneticinvestigations. For example, one may utilize a suitable genetic markerwhich is closely genetically linked to a trait of interest. One of thesemarkers may therefore be used to identify the presence or absence of atrait in the offspring of a particular cross, and hence may be used inselection of progeny for continued breeding. This technique may commonlybe referred to as marker assisted selection. Any other type of geneticmarker or other assay which is able to identify the relative presence orabsence of a trait of interest in a plant may also be useful forbreeding purposes. Exemplary procedures for marker assisted selectionwhich are applicable to the breeding of soybeans are disclosed in U.S.Pat. No. 5,437,697, and U.S. Pat. No. 5,491,081, both of whichdisclosures are specifically incorporated herein by reference in theirentirety. Such methods will be of particular utility in the case ofrecessive traits and variable phenotypes, or where conventional assaysare expensive, time consuming or otherwise disadvantageous. Types ofgenetic markers which could be used in accordance with the inventioninclude, but are not necessarily limited to, Simple Sequence LengthPolymorphisms (SSLPs) (Williams et al., 1990), Randomly AmplifiedPolymorphic DNAs (RAPDs), DNA Amplification Fingerprinting (DAF),Sequence Characterized Amplified Regions (SCARs), Arbitrary PrimedPolymerase Chain Reaction (AP-PCR), Amplified Fragment LengthPolymorphisms (AFLPs) (EP 534 858, specifically incorporated herein byreference in its entirety), and Single Nucleotide Polymorphisms (SNPs)(Wang et al., 1998).

Many qualitative characters also have potential use as phenotype-basedgenetic markers in soybeans; however, some or many may not differ amongvarieties commonly used as parents (Bernard and Weiss, 1973). The mostwidely used genetic markers are flower color (purple dominant to white),pubescence color (brown dominant to gray), and pod color (brown dominantto tan). The association of purple hypocotyl color with purple flowersand green hypocotyl color with white flowers is commonly used toidentify hybrids in the seedling stage. Differences in maturity, height,hilum color, and pest resistance between parents can also be used toverify hybrid plants.

III. Origin and Breeding History of an Exemplary Single Locus ConvertedPlant

It is known to those of skill in the art that, by way of the techniqueof backcrossing, one or more traits may be introduced into a givenvariety while otherwise retaining essentially all of the traits of thatvariety. An example of such backcrossing to introduce a trait into astarting variety is described in U.S. Pat. No. 6,140,556, the entiredisclosure of which is specifically incorporated herein by reference.The procedure described in U.S. Pat. No. 6,140,556 can be summarized asfollows: The soybean variety known as Williams '82 [Glycine max L.Merr.] (Reg. No. 222, PI 518671) was developed using backcrossingtechniques to transfer a locus comprising the Rps₁ gene to the varietyWilliams (Bernard and Cremeens, 1988). Williams '82 is a composite offour resistant lines from the BC₆F₃ generation, which were selected from12 field-tested resistant lines from Williams x Kingwa. The varietyWilliams was used as the recurrent parent in the backcross and thevariety Kingwa was used as the source of the Rps₁ locus. This gene locusconfers resistance to 19 of the 24 races of the fungal agent phytopthorarot.

The F₁ or F₂ seedlings from each backcross round were tested forresistance to the fungus by hypocotyl inoculation using the inoculum ofrace 5. The final generation was tested using inoculum of races 1 to 9.In a backcross such as this, where the desired characteristic beingtransferred to the recurrent parent is controlled by a major gene whichcan be readily evaluated during the backcrossing, it is common toconduct enough backcrosses to avoid testing individual progeny forspecific traits such as yield in extensive replicated tests. In general,four or more backcrosses are used when there is no evaluation of theprogeny for specific traits, such as yield. As in this example, lineswith the phenotype of the recurrent parent may be composited without theusual replicated tests for traits such as yield, protein or oilpercentage in the individual lines.

The variety Williams '82 is comparable to the recurrent parent varietyWilliams in all traits except resistance to phytopthora rot. Forexample, both varieties have a relative maturity of 38, indeterminatestems, white flowers, brown pubescence, tan pods at maturity and shinyyellow seeds with black to light black hila.

IV. Tissue Cultures and In Vitro Regeneration of Soybean Plants

A further aspect of the invention relates to tissue cultures of thesoybean variety designated 0007583. As used herein, the term “tissueculture” indicates a composition comprising isolated cells of the sameor a different type or a collection of such cells organized into partsof a plant. Exemplary types of tissue cultures are protoplasts, calliand plant cells that are intact in plants or parts of plants, such asembryos, pollen, flowers, leaves, roots, root tips, anthers, and thelike. In a preferred embodiment, the tissue culture comprises embryos,protoplasts, meristematic cells, pollen, leaves or anthers.

Exemplary procedures for preparing tissue cultures of regenerablesoybean cells and regenerating soybean plants therefrom, are disclosedin U.S. Pat. No. 4,992,375; U.S. Pat. No. 5,015,580; U.S. Pat. No.5,024,944, and U.S. Pat. No. 5,416,011, each of the disclosures of whichis specifically incorporated herein by reference in its entirety.

An important ability of a tissue culture is the capability to regeneratefertile plants. This allows, for example, transformation of the tissueculture cells followed by regeneration of transgenic plants. Fortransformation to be efficient and successful, DNA must be introducedinto cells that give rise to plants or germ-line tissue.

Soybeans typically are regenerated via two distinct processes; shootmorphogenesis and somatic embryogenesis (Finer, 1996). Shootmorphogenesis is the process of shoot meristem organization anddevelopment. Shoots grow out from a source tissue and are excised androoted to obtain an intact plant. During somatic embryogenesis, anembryo (similar to the zygotic embryo), containing both shoot and rootaxes, is formed from somatic plant tissue. An intact plant rather than arooted shoot results from the germination of the somatic embryo.

Shoot morphogenesis and somatic embryogenesis are different processesand the specific route of regeneration is primarily dependent on theexplant source and media used for tissue culture manipulations. Whilethe systems are different, both systems show variety-specific responseswhere some lines are more responsive to tissue culture manipulationsthan others. A line that is highly responsive in shoot morphogenesis maynot generate many somatic embryos. Lines that produce large numbers ofembryos during an ‘induction’ step may not give rise to rapidly-growingproliferative cultures. Therefore, it may be desired to optimize tissueculture conditions for each soybean line. These optimizations mayreadily be carried out by one of skill in the art of tissue culturethrough small-scale culture studies. In addition to line-specificresponses, proliferative cultures can be observed with both shootmorphogenesis and somatic embryogenesis. Proliferation is beneficial forboth systems, as it allows a single, transformed cell to multiply to thepoint that it will contribute to germ-line tissue.

Shoot morphogenesis was first reported by Wright et al. (1986) as asystem whereby shoots were obtained de novo from cotyledonary nodes ofsoybean seedlings. The shoot meristems were formed subepidermally andmorphogenic tissue could proliferate on a medium containing benzyladenine (BA). This system can be used for transformation if thesubepidermal, multicellular origin of the shoots is recognized andproliferative cultures are utilized. The idea is to target tissue thatwill give rise to new shoots and proliferate those cells within themeristematic tissue to lessen problems associated with chimerism.Formation of chimeras, resulting from transformation of only a singlecell in a meristem, are problematic if the transformed cell is notadequately proliferated and does not does not give rise to germ-linetissue. Once the system is well understood and reproducedsatisfactorily, it can be used as one target tissue for soybeantransformation.

Somatic embryogenesis in soybean was first reported by Christianson etal. (1983) as a system in which embryogenic tissue was initiallyobtained from the zygotic embryo axis. These embryogenic cultures wereproliferative but the repeatability of the system was low and the originof the embryos was not reported. Later histological studies of adifferent proliferative embryogenic soybean culture showed thatproliferative embryos were of apical or surface origin with a smallnumber of cells contributing to embryo formation. The origin of primaryembryos (the first embryos derived from the initial explant) isdependent on the explant tissue and the auxin levels in the inductionmedium (Hartweck et al., 1988). With proliferative embryonic cultures,single cells or small groups of surface cells of the ‘older’ somaticembryos form the ‘newer’ embryos.

Embryogenic cultures can also be used successfully for regeneration,including regeneration of transgenic plants, if the origin of theembryos is recognized and the biological limitations of proliferativeembryogenic cultures are understood. Biological limitations include thedifficulty in developing proliferative embryogenic cultures and reducedfertility problems (culture-induced variation) associated with plantsregenerated from long-term proliferative embryogenic cultures. Some ofthese problems are accentuated in prolonged cultures. The use of morerecently cultured cells may decrease or eliminate such problems.

V. Genetic Transformation of Soybeans

Genetic transformation may be used to insert a selected transgene intothe soybean variety of the invention or may, alternatively, be used forthe preparation of transgenes which can be introduced by backcrossing.Methods for the transformation of many economically important plants,including soybeans, are well know to those of skill in the art.Techniques which may be employed for the genetic transformation ofsoybeans include, but are not limited to, electroporation,microprojectile bombardment, Agrobacterium-mediated transformation anddirect DNA uptake by protoplasts.

To effect transformation by electroporation, one may employ eitherfriable tissues, such as a suspension culture of cells or embryogeniccallus or alternatively one may transform immature embryos or otherorganized tissue directly. In this technique, one would partiallydegrade the cell walls of the chosen cells by exposing them topectin-degrading enzymes (pectolyases) or mechanically wound tissues ina controlled manner.

Protoplasts may also be employed for electroporation transformation ofplants (Bates, 1994; Lazzeri, 1995). For example, the generation oftransgenic soybean plants by electroporation of cotyledon-derivedprotoplasts was described by Dhir and Widholm in Intl. Patent Appl.Publ. No. WO 92/17598, the disclosure of which is specificallyincorporated herein by reference.

A particularly efficient method for delivering transforming DNA segmentsto plant cells is microprojectile bombardment. In this method, particlesare coated with nucleic acids and delivered into cells by a propellingforce. Exemplary particles include those comprised of tungsten,platinum, and preferably, gold. For the bombardment, cells in suspensionare concentrated on filters or solid culture medium. Alternatively,immature embryos or other target cells may be arranged on solid culturemedium. The cells to be bombarded are positioned at an appropriatedistance below the macroprojectile stopping plate.

An illustrative embodiment of a method for delivering DNA into plantcells by acceleration is the Biolistics Particle Delivery System, whichcan be used to propel particles coated with DNA or cells through ascreen, such as a stainless steel or Nytex screen, onto a surfacecovered with target soybean cells. The screen disperses the particles sothat they are not delivered to the recipient cells in large aggregates.It is believed that a screen intervening between the projectileapparatus and the cells to be bombarded reduces the size of projectilesaggregate and may contribute to a higher frequency of transformation byreducing the damage inflicted on the recipient cells by projectiles thatare too large.

Microprojectile bombardment techniques are widely applicable, and may beused to transform virtually any plant species. The application ofmicroprojectile bombardment for the transformation of soybeans isdescribed, for example, in U.S. Pat. No. 5,322,783, the disclosure ofwhich is specifically incorporated herein by reference in its entirety.

Agrobacterium-mediated transfer is another widely applicable system forintroducing gene loci into plant cells. An advantage of the technique isthat DNA can be introduced into whole plant tissues, thereby bypassingthe need for regeneration of an intact plant from a protoplast. ModernAgrobacterium transformation vectors are capable of replication in E.coli as well as Agrobacterium, allowing for convenient manipulations(Klee et al., 1985). Moreover, recent technological advances in vectorsfor Agrobacterium-mediated gene transfer have improved the arrangementof genes and restriction sites in the vectors to facilitate theconstruction of vectors capable of expressing various polypeptide codinggenes. The vectors described have convenient multi-linker regionsflanked by a promoter and a polyadenylation site for direct expressionof inserted polypeptide coding genes. Additionally, Agrobacteriumcontaining both armed and disarmed Ti genes can be used fortransformation.

In those plant strains where Agrobacterium-mediated transformation isefficient, it is the method of choice because of the facile and definednature of the gene locus transfer. The use of Agrobacterium-mediatedplant integrating vectors to introduce DNA into plant cells is wellknown in the art (Fraley et al., 1985; U.S. Pat. No. 5,563,055). Use ofAgrobacterium in the context of soybean transformation has beendescribed, for example, by Chee and Slightom (1995) and in U.S. Pat. No.5,569,834, the disclosures of which are specifically incorporated hereinby reference in their entirety.

Transformation of plant protoplasts also can be achieved using methodsbased on calcium phosphate precipitation, polyethylene glycol treatment,electroporation, and combinations of these treatments (see, e.g.,Potrykus et al., 1985; Omirulleh et al., 1993; Fromm et al., 1986;Uchimiya et al., 1986; Marcotte et al., 1988). The demonstrated abilityto regenerate soybean plants from protoplasts makes each of thesetechniques applicable to soybean (Dhir et al., 1991).

VI. Definitions

In the description and tables which follow, a number of terms are used.In order to provide a clear and consistent understanding of thespecification and claims, the following definitions are provided:

A: When used in conjunction with the word “comprising” or other openlanguage in the claims, the words “a” and “an” denote “one or more.”

Allele: Any of one or more alternative forms of a gene locus, all ofwhich alleles relate to one trait or characteristic. In a diploid cellor organism, the two alleles of a given gene occupy corresponding locion a pair of homologous chromosomes.

Backcrossing: A process in which a breeder repeatedly crosses hybridprogeny, for example a first generation hybrid (F₁), back to one of theparents of the hybrid progeny. Backcrossing can be used to introduce oneor more single locus conversions from one genetic background intoanother.

Brown Stem Rot: This is a visual disease score from 1 to 9 comparing allgenotypes in a given test. The score is based on leaf symptoms ofyellowing and necrosis caused by brown stem rot. A score of 1 indicatesno symptoms. Visual scores range to a score of 9 which indicates severesymptoms of leaf yellowing and necrosis.

Chromatography: A technique wherein a mixture of dissolved substancesare bound to a solid support followed by passing a column of fluidacross the solid support and varying the composition of the fluid. Thecomponents of the mixture are separated by selective elution.

Crossing: The mating of two parent plants.

Cross-pollination: Fertilization by the union of two gametes fromdifferent plants.

Diploid: A cell or organism having two sets of chromosomes.

Emasculate: The removal of plant male sex organs or the inactivation ofthe organs with a cytoplasmic or nuclear genetic factor conferring malesterility or a chemical agent.

Emergence: This is a score indicating the ability of a seed to emergefrom the soil after planting. Each genotype is given a 1 to 9 scorebased on its percent of emergence. A score of 1 indicates an excellentrate and percent of emergence, an intermediate score of 5 indicatesaverage ratings and a 9 score indicates a very poor rate and percent ofemergence.

Enzymes: Molecules which can act as catalysts in biological reactions.

F₁ Hybrid: The first generation progeny of the cross of two nonisogenicplants.

Genotype: The genetic constitution of a cell or organism.

Haploid: A cell or organism having one set of the two sets ofchromosomes in a diploid.

Iron-Deficiency Chlorosis: A plant scoring system ranging from 1 to 9based on visual observations. A score of 1 means no stunting of theplants or yellowing of the leaves and a score of 9 indicates the plantsare dead or dying caused by iron-deficiency chlorosis, a score of 5means plants have intermediate health with some leaf yellowing.

Linkage: A phenomenon wherein alleles on the same chromosome tend tosegregate together more often than expected by chance if theirtransmission was independent.

Lodging Resistance: Lodging is rated on a scale of 1 to 9. A score of 1indicates erect plants. A score of 5 indicates plants are leaning at a45 degree(s) angle in relation to the ground and a score of 9 indicatesplants are laying on the ground.

Marker: A readily detectable phenotype, preferably inherited incodominant fashion (both alleles at a locus in a diploid heterozygoteare readily detectable), with no environmental variance component, i.e.,heritability of 1.

Maturity Date: Plants are considered mature when 95% of the pods havereached their mature color. The maturity date is typically described inmeasured days after August 31 in the northern hemisphere.

Phenotype: The detectable characteristics of a cell or organism, whichcharacteristics are the manifestation of gene expression.

Phytophthora Tolerance: Tolerance to Phytophthora root rot is rated on ascale of 1 to 9, with a score of 1 being the best or highest toleranceranging down to a score of 9, which indicates the plants have notolerance to Phytophthora.

Plant Height: Plant height is taken from the top of soil to the top nodeof the plant and is measured in inches.

Quantitative Trait Loci (QTL): Quantitative trait loci (QTL) refer togenetic loci that control to some degree numerically representabletraits that are usually continuously distributed.

Regeneration: The development of a plant from tissue culture.

Relative Maturity: The maturity grouping designated by the soybeanindustry over a given growing area. This figure is generally dividedinto tenths of a relative maturity group. Within narrow comparisons, thedifference of a tenth of a relative maturity group equates very roughlyto a day difference in maturity at harvest.

Seed Protein Peroxidase Activity. Seed protein peroxidase activity isdefined as a chemical taxonomic technique to separate varieties based onthe presence or absence of the peroxidase enzyme in the seed coat. Thereare two types of soybean varieties, those having high peroxidaseactivity (dark red color) and those having low peroxidase activity (nocolor).

Seed Yield (Bushels/Acre): The yield in bushels/acre is the actual yieldof the grain at harvest.

Self-pollination: The transfer of pollen from the anther to the stigmaof the same plant.

Shattering: The amount of pod dehiscence prior to harvest. Poddehiscence involves seeds falling from the pods to the soil. This is avisual score from 1 to 9 comparing all genotypes within a given test. Ascore of 1 means pods have not opened and no seeds have fallen out. Ascore of 5 indicates approximately 50% of the pods have opened, withseeds falling to the ground and a score of 9 indicates 100% of the podsare opened.

Single Locus Converted (Conversion) Plant: Plants which are developed bya plant breeding technique called backcrossing, wherein essentially allof the desired morphological and physiological characteristics of asoybean variety are recovered in addition to the characteristics of thesingle locus transferred into the variety via the backcrossing techniqueand/or by genetic transformation.

Substantially Equivalent: A characteristic that, when compared, does notshow a statistically significant difference (e.g., p=0.05) from themean.

Tissue Culture: A composition comprising isolated cells of the same or adifferent type or a collection of such cells organized into parts of aplant.

Transgene: A genetic locus comprising a sequence which has beenintroduced into the genome of a soybean plant by transformation.

VII. Deposit Information

A deposit of the soybean variety 0007583, disclosed above and recited inthe claims, has been made with the American Type Culture Collection(ATCC), 10801 University Blvd., Manassas, Va. 20110-2209. The date ofdeposit was Jan. 14, 2004. All restrictions upon the deposit have beenremoved, and the deposit is intended to meet all of the requirements of37 C.F.R. §1.801–1.809. The accession number for those deposited seedsof soybean variety 0007583 is ATCC Accession No. PTA-5764. The depositwill be maintained in the depository for a period of 30 years, or 5years after the last request, or for the effective life of the patent,whichever is longer, and will be replaced if necessary during thatperiod.

REFERENCES

The following references, to the extent that they provide exemplaryprocedural or other details supplementary to those set forth herein, arespecifically incorporated herein by reference.

-   Allard, “Principles of plant breeding,” John Wiley & Sons, NY,    University of California, Davis, Calif., 50–98, 1960.-   Anderson, “Weed science principles,” West Pub. Co., 1983.-   Bates, “Genetic transformation of plants by protoplast    electroporation,” Mol. Biotechnol., 2(2):135–145, 1994.-   Bernard and Cremeens, “Registration of Williams '82 Soybean,” Crop    Sci., 28:1027–1028, 1988.-   Bernard and Weiss, “Qualitative genetics,” In: Soybeans:    Improvement, Production, and Uses, Caldwell (ed), Am. Soc. of    Agron., Madison, Wis., 117–154, 1973.-   Boerma and Moradshahi, “Pollen movement within and between rows to    male-sterile soybeans,” Crop Sci., 15:858–861, 1975.-   Borthwick and Parker, “Photoperiodic perception in Biloxi soybeans,”    Bot. Gaz., 100:374–387, 1938.-   Bowers, Paschall, Bernard, Goodman, “Inheritance of resistance to    soybean mosaic virus in ‘buffalo’ and HLS soybean,” Crop Sci.,    32(1):67–72, 1992.-   Brim and Stuber, “Application of genetic male sterility to recurrent    selection schemes in soybeans,” Crop Sci., 13:528–530, 1973.-   Carlson, “Morphology”, In: Soybeans: Improvement, Production, and    Uses, Caldwell (ed), Am. Soc. of Agron., Madison, Wis., 17–95, 1973.-   Chee and Slightom, “Transformation of soybean (Glycine max) via    Agrobacterium tumefaciens and analysis of transformed plants,”    Methods Mol. Biol., 44:101–119, 1995.-   Christianson, Warnick, Carlson, “A morphogenetically competent    soybean suspension culture,” Science, 222:632–634, 1983.-   Criswell and Hume, “Variation in sensitivity to photoperiod among    early maturing soybean strains,” Crop Sci., 12:657–660, 1972.-   Dhir, Dhir, Sturtevant, Winholm, “Regeneration of transformed shoots    for electroporated soybean Glycine max L. Merr. protoplasts,” Plant    Cell Rep., 10(2):97–101, 1991.-   Fehr, “Soybean,” In: Hybridization of Crop Plants, Fehr and Hadley    (eds), Am. Soc. Agron. and Crop Sci. Soc. Am., Madison, Wis.,    590–599, 1980.-   Fehr, In: “Soybeans: Improvement, Production and Uses,” 2d Ed.,    Manograph 16:249, 1987a.-   Fehr, “Principles of variety development,” Theory and Technique    (Vol 1) and Crop Species Soybean (Vol 2), Iowa State Univ.,    Macmillian Pub. Co., NY, 360–376, 1987b.-   Finer, Cheng, Verma, “Soybean transformation: Technologies and    progress,” In: Soybean: Genetics, Molecular Biology and    Biotechnology, CAB Intl, Verma and Shoemaker (ed), Wallingford,    Oxon, UK, 250–251, 1996.-   Fraley, Rogers, Horsch, Eichholtz, Flick, Fink, Hoffmann, Sanders,    “The sev system a new disarmed ti plasmid vector system for plant    transformation,” Bio. Tech., 3(7):629–635, 1985.-   Fromm, Taylor, Walbot, “Stable transformation of maize after gene    transfer by electroporation,” Nature, 319(6056):791–793., 1986.-   Hamner, “Glycine max(L.) Merrill,” In: The Induction of Flowering:    Some Case Histories, Evans (ed), Cornell Univ. Press, Ithaca, NY,    62–89, 1969.-   Hartweck, Lazzeri, Cui, Collins, Williams “Auxin orientation effects    on somatic embryogenesis from immature soybean cotyledons,” In Vitro    Cell. Develop. Bio., 24:821–828, 1988.-   Johnson and Bernard, “Soybean genetics and breeding,” In: The    Soybean, Norman (ed), Academic Press, NY, 1–73, 1963.-   Kiihl, Hartwig, Kilen, “Grafting as a tool in soybean breeding,”    Crop Sci., 17:181–182, 1977.-   Klee, Yanofsky, Nester, “Vectors for transformation of higher    plants,” Bio. Tech., 3(7):637–642, 1985.-   Kuehl, “Pollen viability and stigma receptivity of Glycine max (L.)    Merrill,” Thesis, North Carolina State College, Raleigh, N.C., 1961.-   Lazzeri, “Stable transformation of barley via direct DNA uptake.    Electroporation- and PEG-mediated protoplast transformation,”    Methods Mol. Biol., 49:95–106, 1995.-   Major, Johnson, Tanner, Anderson, “Effects of daylength and    temperature on soybean development,” Crop Sci., 15:174–179, 1975.-   Marcotte and Bayley, Quatrano, “Regulation of a wheat promoter by    abscisic acid in rice protoplasts,” Nature, 335(6189):454–457, 1988.-   Nickell and Bernard, “Registration of L84-5873 and L84-5932 soybean    germplasm lines resistant to brown stem rot,” Crop Sci., 32(3):835,    1992.-   Omirulleh, Abraham, Golovkin, Stefanov, Karabaev, Mustardy, Morocz,    Dudits, “Activity of a chimeric promoter with the doubled CaMV 35S    enhancer element in protoplast-derived cells and transgenic plants    in maize,” Plant Mol. Biol., 21(3):415–428, 1993.-   Parker, Hendricks, Borthwick, Scully, “Action spectrum for the    photoperiodic control of floral initiation of short-day plants,”    Bot. Gaz., 108:1–26, 1946.-   Poehlman and Sleper, “Breeding Field Crops” Iowa State University    Press, Ames, 1995.-   Potrykus, Paszkowski, Saul, Petruska, Shillito, “Molecular and    general genetics of a hybrid foreign gene introduced into tobacco by    direct gene transfer,” Mol. Gen. Genet., 199(2):169–177, 1985.-   Shanmugasundaram and Tsou, “Photoperiod and critical duration for    flower induction in soybean,” Crop Sci., 18:598–601, 1978.-   Shibles, Anderson, Gibson, “Soybean,” In: Crop Physiology, Some Case    Histories, Evans (ed), Cambridge Univ. Press, Cambridge, England,    51–189, 1975.-   Simmonds, “Principles of crop improvement,” Longman, Inc., NY,    369–399, 1979.-   Sneep and Hendriksen, “Plant breeding perspectives,” Wageningen    (ed), Center for Agricultural Publishing and Documentation, 1979.-   Sprague and Dudley, eds., Corn and Improvement, 3rd ed., 1988.-   Uchimiya, Fushimi, Hashimoto, Harada, Syono, Sugawara, “Expression    of a foreign gene in callus derived from DNA-treated protoplasts of    rice (Oryza-sativa)” Mol. Gen. Genet., 204(2):204–207, 1986.-   van Schaik and Probst, “Effects of some environmental factors on    flower production and reproductive efficiency in soybeans,” Agron.    J, 50:192–197, 1958.-   Walker, Cianzio, Bravo, Fehr, “Comparison of emasculation and    nonemasculation for artificial hybridization of soybeans,” Crop    Sci., 19:285–286, 1979.-   Wang et al., “Large-scale identification, mapping, and genotyping of    single-nucleotide polymorphisms in the human genome,” Science,    280:1077–1082, 1998.-   Williams et al., “Oligonucleotide primers of arbitrary sequence    amplify DNA polymorphisms which are useful as genetic markers,”    Nucleic Acids Res., 18:6531–6535, 1990.-   Wright, Koehler, Hinchee, Cames, “Plant regeneration by    organogenesis in Glycine max,” Plant Cell Reports, 5:150–154, 1986.

1. Soybean seed designated 0007583, wherein a sample of said seed hasbeen deposited under ATCC Accession No. PTA-5764.
 2. A plant produced bygrowing the seed of claim
 1. 3. Pollen of the plant of claim
 2. 4. Anovule of the plant of claim
 2. 5. A cell of the soybean plant of claim2.
 6. A soybean plant having all of the physiological and morphologicalcharacteristics of the plant of claim
 2. 7. A tissue culture ofregenerable cells of the soybean variety 0007583, wherein the tissueculture regenerates soybean plants expressing all the physiological andmorphological characteristics of the soybean variety 0007583 and whereina sample of the seed of said soybean variety 0007583 has been depositedunder ATCC Accession No. PTA-5764.
 8. The tissue culture of claim 7,wherein the regenerable cells are obtained from embryos, meristematiccells, pollen, leaves, roots, root tips or flowers or are protoplasts orcallus derived therefrom.
 9. A soybean plant regenerated from the tissueculture of claim 7, wherein the regenerated soybean plant express allthe physiological and morphological characteristics of the soybeanvariety 0007583, and wherein a sample of the seed of said soybeanvariety 0007583 has been deposited under ATCC Accession No. PTA-5764.10. A method of producing soybean seed, wherein the method comprisescrossing soybean variety 0007583 with itself or a second soybean plant,wherein a sample of the seed of said soybean variety 0007583 has beendeposited under ATCC Accession No. PTA-5764.
 11. The method of claim 10,wherein the method produces a hybrid soybean seed, wherein the methodcomprises crossing the soybean variety 0007583 to a second, distinctsoybean plant, wherein a sample of the seed of said soybean variety0007583 has been deposited under ATCC Accession No. PTA-5764.
 12. Themethod of claim 11, wherein crossing comprises the steps of: (a)planting a seed of soybean variety 0007583 and a second, distinctsoybean plant, wherein a sample of the seed of said soybean variety0007583 has been deposited under ATCC Accession No. PTA-5764; (b)growing soybean plants from said seed until said plants bear flowers;(c) cross pollinating a flower of said soybean variety 0007583 withpollen from said second soybean plant or cross pollinating a flower ofsaid second soybean plant with pollen from said soybean variety 0007583;and (d) harvesting seed resulting from said cross pollinating.
 13. Amale sterile soybean plant produced by transforming the soybean plant ofclaim 2 with a transgene that confers male sterility.
 14. A method ofproducing an herbicide resistant soybean plant wherein the methodcomprises transforming the soybean plant of claim 2 with a transgenethat confers herbicide resistance.
 15. An herbicide resistant soybeanplant produced by the method of claim
 5. 16. A method of producing aninsect resistant soybean plant wherein the method comprises transformingthe soybean plant of claim 2 with a transgene that confers insectresistance.
 17. An insect resistant soybean plant produced by the methodof claim
 16. 18. A method of producing a disease resistant soybean plantwherein the method comprises transforming the soybean plant of claim 2with a transgene that confers disease resistance.
 19. A diseaseresistant soybean plant produced by the method of claim 18.